> Markdown version of [/jobs/ext/2588145-supervisor-data-review](https://www.wearedevelopers.com/jobs/ext/2588145-supervisor-data-review). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Supervisor: Data Review - **Company:** Life Technologies - **Location:** Cincinnati, OH, United States - **Experience:** Experienced - **Contract:** Permanent contract - **Skills:** Microsoft Project, Smartsheet - **Published:** August 14, 2026 - **Apply:** https://www.jobmonkeyjobs.com/career/27931370/Supervisor-Data-Review-Ohio-Cincinnati-7377 ## About the Role * Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in pharmaceutical industry, with focus on R&D, technology transfer, and/or project management * Preferred Fields of Study: Chemistry, Pharmaceutical Technology, Engineering, or related scientific field * PMP certification or equivalent project management certification desirable * 2+ years of supervisory experience or demonstrated team leadership * Strong knowledge of cGMP, pharmaceutical development processes, and regulatory requirements * Experience in managing complex technical projects and client relationships * Expertise in project management methodologies and tools (MS Project, Smartsheet, etc.) Leadership & Communication: * Experience leading, mentoring, and developing teams * Proficiency in stakeholder management and client communication * Effective negotiation and problem-solving capabilities * Ability to manage multiple priorities in a responsive environment Core Competencies: * Advanced English language proficiency * Strong analytical and decision-making skills * Excellent organizational and time management abilities * Proven ability to implement improvement initiatives * Experience with budget management and resource planning Technical Operations: * Proficiency in pharmaceutical production techniques and processes * Experience in technology transfer and scale-up activities * Knowledge of quality systems and compliance requirements * Ability to evaluate technical costs and assess project risks * Understanding of laboratory operations and analytical methods, Must be legally authorized to work in the United States now and in the future, without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. ## Description Join Thermo Fisher Scientific as a Supervisor, R&D Projects, overseeing initiatives that help make the world healthier, cleaner, and safer. In this role, you'll lead a team of project managers and technical specialists while ensuring successful execution of complex pharmaceutical development and technology transfer projects. You'll contribute to innovation by coordinating cross-functional teams, managing resource allocation, and maintaining client relationships. 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